Device recall
Z-1772-2019: Philips IntelliBridge System configured with a regional setting which uses a…
FDA device recall · Class III · Philips North America, LLC
Key facts
| Recall number (Z-number) | Z-1772-2019 |
|---|---|
| Recall event | 82914 |
| Product | Philips IntelliBridge System configured with a regional setting which uses a comma for a decimal separator: 866417 IntelliBridge System C.01 (or later) 866418 IntelliBridge System C.01 upgrade (or later) Product Usage: The IntelliBridge System is indicated for use in data collection and clinical… |
| Recalling firm | Philips North America, LLC |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 22, 2024 |
| FEI number | 1218950 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database